Methanol Synthesis in a Slurry Phase Reactor over Cu/ZnO/Al2O3 Catalyst

2014 ◽  
Vol 931-932 ◽  
pp. 27-31 ◽  
Author(s):  
Kuntima Krekkeitsakul ◽  
Thanes Utistham ◽  
Unalome Wetwatana Hartley

Methanol synthesis from synthesis gas (syngas, a mixture of hydrogen (H2) and carbon monoxide (CO)) in the presence of copper/zinc oxide/alumina catalyst (Cu/ZnO/Al2O3) was investigated using semi-batch reactor. The process was operated at 280 °C under pressure 40 bar in a slurry reactor (Parr reactor model 4848). The catalyst weight, syngas molar ratio and residence time were optimized for methanol synthesis. Cu/ZnO/Al2O3catalyst was prepared by a two-step surfactant assisted precipitation method using polyethylene glycol (PEG 6000). The catalysts surface area, crystallinity, reducibility and morphology were characterized by BET, XRD, H2-TPR and SEM-EDS, respectively. The BET analysis indicated that the catalyst calcined at 300 °C gave the highest surface area (99.67 m2/g). The crystallite size of Cu in Cu/ZnO/Al2O3catalyst was estimated to be 14.14 nm., after adding the surfactants. The maximum methanol yield (607.53) was achieved after 24 hours of residence time using 5 g of the catalyst under a stream of 2 to 1 molar ratio of H2and CO reactive mixed gas. Under these conditions, 38.26% of CO conversion and 93.11% of selectivity to methanol were achieved. When the residence time was decreased to 12 hours with molar ratio of 0.5 H2to 1 CO, the yield of methanol was 388.11, with a CO conversion of 38.53% and selectivity to methanol of 90.77%.

2020 ◽  
Vol 13 (2) ◽  
Author(s):  
Ade Syafrinaldy ◽  
Zulaicha Dwi Hastuti

This research is aiming to formulate the most appropriate catalyst which is expected to be able to directthe reaction to form Dimethyl Ether (DME) in direct synthesis process using dual catalyst. It iscommonly known that DME can be formulated from synthetic gasses reaction, H2 and CO. Theprocess might be gone through indirect synthesis, methanol synthesis and dehydration, or directsynthesis in which both rections take place in one reactor. Both processes, indirect or direct synthesis,each would be needed the right catalyst. Dual catalyst is prepared by mixing physically methanolsynthesis catalyst and methanol dehydration to form DME.As methanol dehydration catalyst, we makeuse of HZSM-5 with Si/Al ratio of 25 and 90. This HZSM-5 is firstly calcined for 6 hours at 500°C. Thetemperature is raised to 500°C from ambient with pace of 5°C/min. The methanol synthesis catalyst isbased on CuZnAl, made by copresipitation method from Cu(NO3)2.3H2O; Zn(NO3)2.4H2O andAl(NO3)2.9H2O. The catalyst was then calcined at 350 ° C for 6 hours, then reduced by hydrogen 10 ml /minute and nitrogen 90 ml / min at 240 ° C, atmospheric pressure for 10 hours to remove the Ocomponent in the catalyst. The catalyst that has been prepared is CuZnAl with a ratio of 4: 3: 1; 5: 3: 1and 6: 3: 1. The ratio of the two catalysts is 2: 1 for Cu / Zn / Al2O3: HZSM-5. The catalytic activity test iscarried out using a continuous tubular fixed-bed microactivity reactor. The reaction is carried out at apressure between 3 - 4 MPa and a temperature in the range of 200 - 300 ° C. T The flow rate of thereactant gas is controlled by a mass flow controller, with a mass of 1 g of catalyst. Through the catalyticactivity test, the best methanol synthesis was given by CuZnAl catalyst with a 5: 3: 1 molar ratio, whichresulted in a CO conversion of 19.66% greater than the commercial catalyst of CZA-Sudchemie of15.62%. As for dehydration of methanol, the best result was given by Sudchemie-ZSM-5 catalyst withSi /Al 25 ratio resulting in higher DME concentration (0.90%) than Si /Al 90 ratio (0.45%).Keywords : direct synthesis, methanol synthesis, methanol dehydration, dual catalyst, CO conversion


Author(s):  
A. V. Sulimov ◽  
A. V. Ovcharova ◽  
G. M. Kravchenko ◽  
Yu. K. Sulimova

Objectives. Cyclic carbonates are important products of organic synthesis, which are widely used as solvents, catalysts, and reagents for the production of various compounds (in particular, urethane-containing polymers) by the non-isocyanate method. The process of carbamide alcoholysis with polybasic alcohols is a promising method for the synthesis of cyclic carbonates. The purpose of this study is to determine the reaction conditions for the interaction of propylene glycol with carbamide in the presence of zinc acetate as a catalyst.Methods. We conducted experiments to study the synthesis of propylene carbonate in a batch laboratory apparatus. Moreover, we analyzed the starting reagents and final products using gas–liquid chromatography.Results. We studied the synthesis of propylene carbonate by carbamide alcoholysis with propylene glycol in the presence of a catalyst (zinc acetate) by varying the following parameters: initial molar ratio of propylene glycol/carbamide = (0.5–5):1, synthesis temperature 130–190°С, reagent residence time in the reactor 0.5–4 h, and the catalyst amount in the reaction mixture 0–1.5 wt %.Conclusions. We determined the technological parameters of propylene carbonate synthesis in a batch reactor. Moreover, we showed that the process allowed the production of propylene carbonate with a sufficiently high yield of 80%—at the initial molar ratio of propylene glycol/ carbamide = 3:1, temperature 170°C, and residence time 2 h.


2018 ◽  
Vol 127 (1A) ◽  
pp. 15
Author(s):  
Ngô Minh Đức

Hydrotalcite was synthesized using the co-precipitation method with  the Mg/Al molar ratio of 3.0 and then  calcined at 450 °C, for 5 h. The obtained solid was characterized by XRD, BET. As seen from results of physical characterization, the synthesized Hydrotalcite material owns large surface area of  309.3 m<sup>2</sup>/g, mean capillary diameter of 11.52 nm. Hydrotalcite application as adsorbent of heavy metal ions. The results of adsorption experiment for Pb<sup>2+</sup> in water showed that the absorption equilibrium was attained after 90 minutes at pH = 5 with maximum adsorption loading capacity of 144.93 mg/g. The synthesized adsorbent could be regenerated with HNO<sub>3</sub> (1M) solution


2014 ◽  
Vol 556-562 ◽  
pp. 117-122 ◽  
Author(s):  
Miao Yao Jia ◽  
Wen Gui Gao ◽  
Hua Wang ◽  
Yu Hao Wang

Various CuO-ZnO-ZrO2(CZZ) catalysts for methanol synthesis from CO2 hydrogenation were prepared by co-precipitation method. Small amount of silica was incorporated into CZZ catalyst to produce these modified ternary CZZ catalysts. The effects of silica on physicochemical and catalytic properties were studied by TG-DTG,XRD,BET,N2O chemisorption,H2-TPR,NH3-TPD and CO2-TPD techniques. The results show that the properties of catalysts were strongly influenced by the content of SiO2 used as promoter. The catalytic performance for methanol synthesis from CO2 hydrogenation was evaluated. The test results show that the CZZ catalyst modified with 4 wt.% SiO2 exhibits an optimum catalytic activity. The silica improves the dispersion of CuO and its modified CZZ catalysts exhibits higher specific surface area, which were confirmed to be responsible for excellent performance of the catalysts for methanol synthesis from CO2 hydrogenation.


2011 ◽  
Vol 399-401 ◽  
pp. 1425-1428
Author(s):  
Jun Zeng ◽  
Feng Chun Zeng ◽  
Jun Bo Zhong ◽  
Jian Zhang Li ◽  
Shao Hua Wang ◽  
...  

In this paper, Bi2O3 and Fe3+-doped Bi2O3 photocatalysts with different molar ratio of Bi /Fe (nBi:nFe =100:1,2,3,4) was prepared by paralled flaw co-precipitation method. The prepared photocatalysts were characterized by Brunauer-Emmet Teller (BET) method, X-ray diffraction( XRD) and UV-Vis diffuse reflectance spectroscopy. The results show that 3% Fe3+-Bi2O3 prepared has the highest BET surface area, pore volume, the smallest pore size and the particle average size. 3% Fe3+-Bi2O3 exhibits the best photocatalytic activity. The results of further experiments show that the specific surface area, UV-Vis diffuse reflectance all play an important role in promotion of photocatalytic activity of Bi2O3 nanostructure.


2018 ◽  
Vol 7 (2) ◽  
pp. 136-141
Author(s):  
Nuni Widiarti ◽  
Ismi Arinal Haq ◽  
F. Widhi Mahatmanti ◽  
Harjito Harjito ◽  
Cepi Kurniawan ◽  
...  

CaO is a very good catalyst for oil transesterification reactions into biodiesel, but requires a reaction time of 2 hours to obtain equilibrium. The time of CaO catalysis reaction can be accelerated by modifying the CaO catalyst with SrO. Synthesis biodiesel of waste cooking oil has been successfully conducted by transesterification reaction that used batch reactor assisted by CaO.SrO catalyst. The aim of this study is to determine the characteristics and catalytic activity of catalyst in the transesterification reaction. Catalysts have been successfully synthesized by coprecipitation method with oil to methanol molar ratio of 1:1, and its calcined at 800oC for 3 hours. Catalyst was characterized by XRD to determine the crystallinity. The smaller catalyst crystallinity obtained as the decline in intensity and shifts diffraction angles of CaO modified SrO catalyst. Surface area of catalyst characterized by SAA, that allow surface area between CaO modified SrO by 10.217 m2/g. Transesterification reaction performed on variation time (30, 60, 90, 120, 150 minutes), and the catalysts amount (1, 2, 4, 6, 8% w/v). The optimum condition of catalytic activity in reaction for 2 hours and the catalyst amount is 1% w/v of reactants that produce yield of biodiesel is 96.4%.


2020 ◽  
Vol 36 (6) ◽  
pp. 1049-1065
Author(s):  
Ravindra Haribhau Waghchaure ◽  
Prashant bhimrao Kol ◽  
Vishnu Ashok Adole ◽  
Bapusonu Jagdale ◽  
Thansing bhavsing Pawar

Zinc oxide is known as multifaceted material due to its special physical and chemical properties. Present research deals with the fabrication of undopedZnO, 1.5% Fe3+ doped ZnO, and 1.5% Ni2+ doped ZnOnanoparticles by low-cost co-precipitation method. These prepared materials were utilized to prepare thick film sensorsby employing a screen printing technique.The structuralconfirmations of these materials wereperformed by various nano-characterization techniques. The structural properties were investigated by XRD to confirm the nanoscaleZnO as well as the average crystal dimensions. The surface morphological properties of undoped and modified ZnO wereanalyzedby SEM and TEM methods. The average volume pores over prepared materials and surface area were concluded from the N2 adsorption-desorption experiment (BET analysis). The Fe3+ doped ZnO has the highest surface area among all the prepared sensors i.e. 23.55 m²/g. The Fe3+ doped ZnO and Ni2+ZnOnanomaterials were observed to show declined band gaps in comparison to the undoped ZnO material. All the prepared sensors were employed for the gas sensing study of gases like NH3, LPG, formaldehyde vapors, toluene vapors, CO, CO2, and NO2. The CO2 and NH3vapors found to be very sensitive towards Fe3+ doped ZnO with 76.62% and 76.58% sensitivity respectively. TheNi2+ doped ZnO sensor sensitivity for CO2 and NH3was recorded as71.20% and 70.23% respectively. The LPG, CH2O, and toluene vapors' sensitivity was also studied for the modified ZnO sensor. Besides, modified ZnO utilized as a relative humidity sensor with an RH variation of 10-90%. The impedance versus humidity curves recorded for all sensors.The Fe3+ doped ZnOnanomaterial at 10Hz was found to be an effective humidity sensor. Theresponse and recovery were found to be very rapid in Fe3+ doped ZnO for NH3, CO2, NO2, and LPGvapors.


2011 ◽  
Vol 233-235 ◽  
pp. 1552-1555
Author(s):  
Yun Peng Zhao ◽  
Li Hua Jia ◽  
Tao Jing ◽  
De Zhi Sun ◽  
Jong Shik Chung

CuO-ZnO-ZrO2-TiO2 catalyst was prepared by parallel-slurry-mixing-precipitation method combined with addition of surfactant. The catalyst characterizations were investigated by Nitrogen adsorption-desorption, XRD, SEM and EDS. Results show that the average pore diameter of the mesoporous CuO-ZnO-ZrO2-TiO2 catalyst is 3.754 nm, and dispersion of CuOis better on CuO-ZnO-ZrO2-TiO2 catalyst. Under the conditions of reaction temperature of 503 K, reaction pressure of 2.0 MPa, space velocity of 2100 h-1 with a H2/CO2 molar ratio of 3:1, the catalyst exhibited favorable activity for methanol synthesis from CO2 hydrogenation. The selectivity to methanol and the yield of methanol were 27.42% and 4.50%, respectively.


2011 ◽  
Vol 493-494 ◽  
pp. 746-751 ◽  
Author(s):  
M. Raz ◽  
F. Moztarzadeh ◽  
A.Ansari Hamedani ◽  
M. Ashuri ◽  
M. Tahriri

In this study, magnetite (Fe3O4) nanoparticles were synthesized at room temperature using FeCl3.6H2O (1.28 M), FeCl2.4H2O (0.64 M) and HCl (0.4 M) for preparing a solution as the iron source and NaOH (0.9-1.5 M) for to prepare a solution as the alkali source by the aqueous phase co-precipitation method under vigorous mechanical stirring (450 and 750 rpm) together with N2 gas flowing through the reaction medium during synthesis operation in closed system. The powder samples were characterized by the commonly used techniques of scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transform infra-red (FTIR), X-ray diffraction (XRD), vibrating sample magnetometry (VSM) and BET analyses. SEM was used to observe the morphology and agglomeration state of the powder. Size and morphology of the precipitated crystallites were examined with TEM. The prevalence of functional groups in the synthesized powders was ascertained by FTIR spectroscopy. The pure magnetite and other phases according to processing parameters were observed by XRD analysis. The magnetic properties of magnetite (Fe3O4) nanoparticles were examined using VSM. Finally, the specific surface area of nanoparticles was measured by BET technique. The results indicate that smaller particles can be synthesized by increasing stirring rate and decreasing the NaOH concentration, which in this case corresponded to 35 nm using 0.9 M NaOH at 750 rpm. The VSM analysis showed a saturation magnetization range of (82-96 emu/g) and coercivity of (83-119 Oe) for particles between (35-96 nm) respectively. Also, the highest specific surface area of 40 m2/g was obtained at 0.9 M NaOH at 750 rpm and the smallest value of 15 m2/g at 1.5 M of NaOH at 450 rpm using BET analysis.


2020 ◽  
Vol 2020 ◽  
pp. 1-14
Author(s):  
Thi Anh Tuyet Pham ◽  
Van Anh Tran ◽  
Van Duong Le ◽  
Minh Viet Nguyen ◽  
Duc Duc Truong ◽  
...  

Zinc oxide (ZnO) has been known as an excellent photocatalyst for the degradation of a variety of organic pollutants under UV irradiation. This work describes a synthesis of ZnO nanoparticles via a facile precipitation method, and Ag was doped into Ag/ZnO nanocomposite to improve the photocatalytic degradation of BPA under visible light irradiation. The obtained ZnO nanoparticles were 20 nm in size and had a relatively high surface area and pore volume, 26.2 m2/g and 0.48 cm3/g, respectively. The deposition of Ag led to a decrease in the surface area, pore volume, and band gap energy ( E g ) of ZnO nanoparticles. However, the photocatalytic activity of Ag/ZnO composite in the case increased. The performance of ZnO was compared with Ag/ZnO composites at the different molar ratios, and the kinetic reaction of BPA in these catalysts was investigated by the first-order kinetic model. The sample of Ag/ZnO-10 composite had the highest catalytic activity and showed the degradation efficiency, reaction rate, and degradation capacity of 100% in 120 min, 0.014 min-1, and 40 mg/g, respectively. In comparison, the effects of Ag/ZnO molar ratio, catalyst dosage, solution pH, and concentration of BPA on photocatalytic degradation were investigated. Additionally, the photocatalytic performance of Ag/ZnO-10 composite was evaluated by the degradation of other persistent organic compounds such as phenol, tartrazine, and methylene blue and compared to other catalysts in literature.


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